* We recommend a score >= 0.08 for meaningful Gene-Disease associations

GeneID	Gene_Symbol	DisGeNet_diseaseID	Disease_name	DisGeNet score	DisGeNet_sourceDB
52	ACP1	C0036341	Schizophrenia	0.200549453568426	BEFREE;PSYGENET
52	ACP1	C0041696	Unipolar Depression	0.200274726784213	BEFREE;PSYGENET
52	ACP1	C1269683	Major Depressive Disorder	0.200274726784213	BEFREE;PSYGENET
52	ACP1	C0011854	Diabetes Mellitus, Insulin-Dependent	0.0250254906547791	BEFREE;GAD
52	ACP1	C0028754	Obesity	0.0145076836743579	BEFREE;GAD
52	ACP1	C0011860	Diabetes Mellitus, Non-Insulin-Dependent	0.0104522944457913	BEFREE;GAD
52	ACP1	C0041296	Tuberculosis	0.0102287248188909	BEFREE;GAD;LHGDN
52	ACP1	C0000786	Spontaneous abortion	0.0078728534529155	GAD;LHGDN
52	ACP1	C0009375	Colonic Neoplasms	0.0078728534529155	GAD;LHGDN
52	ACP1	C0004364	Autoimmune Diseases	0.0076923499579668	BEFREE
52	ACP1	C0020517	Hypersensitivity	0.007221085569864	GAD
52	ACP1	C0004096	Asthma	0.0059129641834284	BEFREE;GAD
52	ACP1	C0014175	Endometriosis	0.00541466777231485	BEFREE;GAD;LHGDN
52	ACP1	C1956346	Coronary Artery Disease	0.0053635106150022	BEFREE;GAD
52	ACP1	C0040517	Gilles de la Tourette syndrome	0.004814057046576	GAD
52	ACP1	C0024141	Lupus Erythematosus, Systemic	0.0037806624443535	BEFREE;GAD
52	ACP1	C0003873	Rheumatoid Arthritis	0.0035714481947703	BEFREE
52	ACP1	C0028326	Noonan Syndrome	0.0032967214105572	BEFREE
52	ACP1	C0041409	Turner Syndrome, Male	0.0032967214105572	BEFREE
52	ACP1	C0006142	Malignant neoplasm of breast	0.0030219946263441	BEFREE
52	ACP1	C0678222	Breast Carcinoma	0.0030219946263441	BEFREE
52	ACP1	C0027819	Neuroblastoma	0.00300763924902685	BEFREE;LHGDN
52	ACP1	C0007222	Cardiovascular Diseases	0.0026817553075011	BEFREE;GAD
52	ACP1	C0010054	Coronary Arteriosclerosis	0.0026817553075011	BEFREE;GAD
52	ACP1	C0023267	Fibroid Tumor	0.0026817553075011	BEFREE;GAD
52	ACP1	C0376358	Malignant neoplasm of prostate	0.0024725410579179	BEFREE
52	ACP1	C0596263	Carcinogenesis	0.0024725410579179	BEFREE
52	ACP1	C0600139	Prostate carcinoma	0.0024725410579179	BEFREE
52	ACP1	C0014548	Epilepsy, Generalized	0.002407028523288	GAD
52	ACP1	C0014549	Tonic-Clonic Epilepsy	0.002407028523288	GAD
52	ACP1	C0021655	Insulin Resistance	0.002407028523288	GAD
52	ACP1	C0023891	Liver Cirrhosis, Alcoholic	0.002407028523288	GAD
52	ACP1	C0024530	Malaria	0.002407028523288	GAD
52	ACP1	C0029458	Osteoporosis, Postmenopausal	0.002407028523288	GAD
52	ACP1	C0040336	Tobacco Use Disorder	0.002407028523288	GAD
52	ACP1	C0042138	Uterine Neoplasms	0.002407028523288	GAD
52	ACP1	C0085207	Gestational Diabetes	0.002407028523288	GAD
52	ACP1	C0010346	Crohn Disease	0.0019230874894917	BEFREE
52	ACP1	C0011847	Diabetes	0.0019230874894917	BEFREE
52	ACP1	C0011849	Diabetes Mellitus	0.0019230874894917	BEFREE
52	ACP1	C0023418	leukemia	0.0019230874894917	BEFREE
52	ACP1	C0027627	Neoplasm Metastasis	0.0016483607052786	BEFREE
52	ACP1	C0017636	Glioblastoma	0.0013736339210655	BEFREE
52	ACP1	C0018213	Graves Disease	0.0008241803526393	BEFREE
52	ACP1	C0021390	Inflammatory Bowel Diseases	0.0008241803526393	BEFREE
52	ACP1	C0178468	Autoimmune thyroid disease	0.0008241803526393	BEFREE
52	ACP1	C0699790	Colon Carcinoma	0.0008241803526393	BEFREE
52	ACP1	C2239176	Liver carcinoma	0.0008241803526393	BEFREE
52	ACP1	C0007102	Malignant tumor of colon	0.0005494535684262	BEFREE
52	ACP1	C0007137	Squamous cell carcinoma	0.0005494535684262	BEFREE
52	ACP1	C0009319	Colitis	0.0005494535684262	BEFREE
52	ACP1	C0009404	Colorectal Neoplasms	0.0005494535684262	BEFREE
52	ACP1	C0021053	Immune System Diseases	0.0005494535684262	BEFREE
52	ACP1	C0023467	Leukemia, Myelocytic, Acute	0.0005494535684262	BEFREE
52	ACP1	C0025202	melanoma	0.0005494535684262	BEFREE
52	ACP1	C0026764	Multiple Myeloma	0.0005494535684262	BEFREE
52	ACP1	C0026769	Multiple Sclerosis	0.0005494535684262	BEFREE
52	ACP1	C0175704	LEOPARD Syndrome	0.0005494535684262	BEFREE
52	ACP1	C0235974	Pancreatic carcinoma	0.0005494535684262	BEFREE
52	ACP1	C0242379	Malignant neoplasm of lung	0.0005494535684262	BEFREE
52	ACP1	C0280100	solid tumor	0.0005494535684262	BEFREE
52	ACP1	C0346647	Malignant neoplasm of pancreas	0.0005494535684262	BEFREE
52	ACP1	C0598766	Leukemogenesis	0.0005494535684262	BEFREE
52	ACP1	C0684249	Carcinoma of lung	0.0005494535684262	BEFREE
52	ACP1	C0751356	Idiopathic Inflammatory Myopathies	0.0005494535684262	BEFREE
52	ACP1	C0751778	Myoclonic Epilepsies, Progressive	0.0005494535684262	BEFREE
52	ACP1	C0751783	Lafora Disease	0.0005494535684262	BEFREE
52	ACP1	C1306460	Primary malignant neoplasm of lung	0.0005494535684262	BEFREE
52	ACP1	C1621958	Glioblastoma Multiforme	0.0005494535684262	BEFREE
52	ACP1	C1961099	Precursor T-Cell Lymphoblastic Leukemia-Lymphoma	0.0005494535684262	BEFREE
52	ACP1	C3539878	Triple Negative Breast Neoplasms	0.0005494535684262	BEFREE
52	ACP1	C3539909	Allergic disposition	0.0005494535684262	BEFREE
52	ACP1	C0001418	Adenocarcinoma	0.0002747267842131	BEFREE
52	ACP1	C0001849	AIDS Dementia Complex	0.0002747267842131	BEFREE
52	ACP1	C0002893	Refractory anemias	0.0002747267842131	BEFREE
52	ACP1	C0002895	Anemia, Sickle Cell	0.0002747267842131	BEFREE
52	ACP1	C0005806	Blood Group Incompatibility	0.0002747267842131	BEFREE
52	ACP1	C0007095	Carcinoid Tumor	0.0002747267842131	BEFREE
52	ACP1	C0007131	Non-Small Cell Lung Carcinoma	0.0002747267842131	BEFREE
52	ACP1	C0008073	Developmental Disabilities	0.0002747267842131	BEFREE
52	ACP1	C0009324	Ulcerative Colitis	0.0002747267842131	BEFREE
52	ACP1	C0009691	Congenital cataract	0.0002747267842131	BEFREE
52	ACP1	C0010068	Coronary heart disease	0.0002747267842131	BEFREE
52	ACP1	C0013336	Dwarfism	0.0002747267842131	BEFREE
52	ACP1	C0014060	Encephalitis, St. Louis	0.0002747267842131	BEFREE
52	ACP1	C0015625	Fanconi Anemia	0.0002747267842131	BEFREE
52	ACP1	C0015702	Favism	0.0002747267842131	BEFREE
52	ACP1	C0017638	Glioma	0.0002747267842131	BEFREE
52	ACP1	C0018553	Hamartoma Syndrome, Multiple	0.0002747267842131	BEFREE
52	ACP1	C0018798	Congenital Heart Defects	0.0002747267842131	BEFREE
52	ACP1	C0021294	Infant, Premature	0.0002747267842131	BEFREE
52	ACP1	C0021670	insulinoma	0.0002747267842131	BEFREE
52	ACP1	C0022665	Kidney Neoplasm	0.0002747267842131	BEFREE
52	ACP1	C0023434	Chronic Lymphocytic Leukemia	0.0002747267842131	BEFREE
52	ACP1	C0023473	Myeloid Leukemia, Chronic	0.0002747267842131	BEFREE
52	ACP1	C0024131	Lupus Vulgaris	0.0002747267842131	BEFREE
52	ACP1	C0024138	Lupus Erythematosus, Discoid	0.0002747267842131	BEFREE
52	ACP1	C0024299	Lymphoma	0.0002747267842131	BEFREE
52	ACP1	C0025286	Meningioma	0.0002747267842131	BEFREE
52	ACP1	C0026896	Myasthenia Gravis	0.0002747267842131	BEFREE
52	ACP1	C0029463	Osteosarcoma	0.0002747267842131	BEFREE
52	ACP1	C0030499	Parasitic Diseases	0.0002747267842131	BEFREE
52	ACP1	C0033860	Psoriasis	0.0002747267842131	BEFREE
52	ACP1	C0034152	Henoch-Schoenlein Purpura	0.0002747267842131	BEFREE
52	ACP1	C0036421	Systemic Scleroderma	0.0002747267842131	BEFREE
52	ACP1	C0037274	Dermatologic disorders	0.0002747267842131	BEFREE
52	ACP1	C0042133	Uterine Fibroids	0.0002747267842131	BEFREE
52	ACP1	C0042900	Vitiligo	0.0002747267842131	BEFREE
52	ACP1	C0079744	Diffuse Large B-Cell Lymphoma	0.0002747267842131	BEFREE
52	ACP1	C0085413	Polycystic Kidney, Autosomal Dominant	0.0002747267842131	BEFREE
52	ACP1	C0085580	Essential Hypertension	0.0002747267842131	BEFREE
52	ACP1	C0085652	Pyoderma Gangrenosum	0.0002747267842131	BEFREE
52	ACP1	C0085669	Acute leukemia	0.0002747267842131	BEFREE
52	ACP1	C0178874	Tumor Progression	0.0002747267842131	BEFREE
52	ACP1	C0205734	Diabetes, Autoimmune	0.0002747267842131	BEFREE
52	ACP1	C0220621	pediatric acute myeloblastic leukemia	0.0002747267842131	BEFREE
52	ACP1	C0221238	Mesangial proliferative glomerulonephritis	0.0002747267842131	BEFREE
52	ACP1	C0238462	Medullary carcinoma of thyroid	0.0002747267842131	BEFREE
52	ACP1	C0242339	Dyslipidemias	0.0002747267842131	BEFREE
52	ACP1	C0265234	Branchio-Oto-Renal Syndrome	0.0002747267842131	BEFREE
52	ACP1	C0266617	Congenital anomaly of face	0.0002747267842131	BEFREE
52	ACP1	C0268575	Isovaleryl-CoA dehydrogenase deficiency	0.0002747267842131	BEFREE
52	ACP1	C0270549	Generalized Anxiety Disorder	0.0002747267842131	BEFREE
52	ACP1	C0271650	Impaired glucose tolerance	0.0002747267842131	BEFREE
52	ACP1	C0272285	Heparin-induced thrombocytopenia	0.0002747267842131	BEFREE
52	ACP1	C0279702	Conventional (Clear Cell) Renal Cell Carcinoma	0.0002747267842131	BEFREE
52	ACP1	C0333307	Superficial ulcer	0.0002747267842131	BEFREE
52	ACP1	C0340288	Stable angina	0.0002747267842131	BEFREE
52	ACP1	C0342276	Maturity onset diabetes mellitus in young	0.0002747267842131	BEFREE
52	ACP1	C0349639	Juvenile Myelomonocytic Leukemia	0.0002747267842131	BEFREE
52	ACP1	C0374997	Helicobacter pylori (H. pylori) infection in conditions classified elsewhere and of unspecified site	0.0002747267842131	BEFREE
52	ACP1	C0409974	Lupus Erythematosus	0.0002747267842131	BEFREE
52	ACP1	C0424295	Hyperactive behavior	0.0002747267842131	BEFREE
52	ACP1	C0476089	Endometrial Carcinoma	0.0002747267842131	BEFREE
52	ACP1	C0524620	Metabolic Syndrome X	0.0002747267842131	BEFREE
52	ACP1	C0545044	Acrokeratoelastoidosis of Costa	0.0002747267842131	BEFREE
52	ACP1	C0549473	Thyroid carcinoma	0.0002747267842131	BEFREE
52	ACP1	C0585442	Osteosarcoma of bone	0.0002747267842131	BEFREE
52	ACP1	C0677607	Hashimoto Disease	0.0002747267842131	BEFREE
52	ACP1	C0677886	Epithelial ovarian cancer	0.0002747267842131	BEFREE
52	ACP1	C0700095	Central neuroblastoma	0.0002747267842131	BEFREE
52	ACP1	C0852733	Completed Suicide	0.0002747267842131	BEFREE
52	ACP1	C0920350	Autoimmune thyroiditis	0.0002747267842131	BEFREE
52	ACP1	C1292778	Chronic myeloproliferative disorder	0.0002747267842131	BEFREE
52	ACP1	C1368683	Epithelioma	0.0002747267842131	BEFREE
52	ACP1	C1458155	Mammary Neoplasms	0.0002747267842131	BEFREE
52	ACP1	C1527249	Colorectal Cancer	0.0002747267842131	BEFREE
52	ACP1	C1739108	Latent Autoimmune Diabetes in Adults	0.0002747267842131	BEFREE
52	ACP1	C1762616	Meningioma, benign, no ICD-O subtype	0.0002747267842131	BEFREE
52	ACP1	C1847835	VITILIGO-ASSOCIATED MULTIPLE AUTOIMMUNE DISEASE SUSCEPTIBILITY 1 (finding)	0.0002747267842131	BEFREE
52	ACP1	C1857276	Trichohepatoenteric Syndrome	0.0002747267842131	BEFREE
52	ACP1	C2939465	Deficiency of glucose-6-phosphate dehydrogenase	0.0002747267842131	BEFREE
52	ACP1	C3469521	FANCONI ANEMIA, COMPLEMENTATION GROUP A (disorder)	0.0002747267842131	BEFREE
52	ACP1	C3495559	Juvenile arthritis	0.0002747267842131	BEFREE
52	ACP1	C3665488	Familial Osteochondritis Dissecans	0.0002747267842131	BEFREE
52	ACP1	C3887505	DYSFUNCTION - SKIN DISORDERS	0.0002747267842131	BEFREE
52	ACP1	C3888318	Myopathy, familial idiopathic inflammatory	0.0002747267842131	BEFREE
52	ACP1	C3899278	Early Rheumatoid Arthritis	0.0002747267842131	BEFREE